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Lynn P Chorich

Showing results (1-10 of 27) with videos related to

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F&S Science|July 29, 2023
Investigation of subfertility in the female Nsmf knockout mouseErica D Louden, Michael P Dougherty, Lynn P Chorich, et al.
Molecular and Cellular Endocrinology|October 21, 2017
JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neuronsEun Kyung Ko, Lynn P Chorich, Megan E Sullivan, et al.
F&S Science|June 28, 2024
Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender womenJohn G Theisen, Lynn P Chorich, Hongyan Xu, et al.
Molecular Human Reproduction|May 9, 2008
The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeJennifer R Pedersen-White, Lynn P Chorich, David P Bick, et al.
Human Genetics|February 3, 2026
Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeDina Kira, Soumia Brakta, Hyung Goo Kim, et al.
Fertility and Sterility|March 8, 2013
Identification of HESX1 mutations in Kallmann syndromeKayce Newbern, Nithya Natrajan, Hyung-Goo Kim, et al.
The New England Journal of Medicine|July 12, 2013
Delayed puberty and estrogen resistance in a woman with estrogen receptor α variantSamuel D Quaynor, Earl W Stradtman, Hyung-Goo Kim, et al.
American Journal of Obstetrics and Gynecology|April 23, 2005
Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarraysNing Xu, Robert H Podolsky, Pranav Chudgar, et al.
Journal of Assisted Reproduction and Genetics|December 23, 2025
The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndromeJaclyn M Kwal, Lynn P Chorich, Anna Navitski, et al.
Scientific Reports|December 29, 2019
The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic VariantsJ Graham Theisen, Viji Sundaram, Mary S Filchak, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
F&S Science|July 29, 2023
Investigation of subfertility in the female Nsmf knockout mouseErica D Louden, Michael P Dougherty, Lynn P Chorich, et al.
Molecular and Cellular Endocrinology|October 21, 2017
JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neuronsEun Kyung Ko, Lynn P Chorich, Megan E Sullivan, et al.
F&S Science|June 28, 2024
Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender womenJohn G Theisen, Lynn P Chorich, Hongyan Xu, et al.
Molecular Human Reproduction|May 9, 2008
The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeJennifer R Pedersen-White, Lynn P Chorich, David P Bick, et al.
Human Genetics|February 3, 2026
Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeDina Kira, Soumia Brakta, Hyung Goo Kim, et al.
Fertility and Sterility|March 8, 2013
Identification of HESX1 mutations in Kallmann syndromeKayce Newbern, Nithya Natrajan, Hyung-Goo Kim, et al.
The New England Journal of Medicine|July 12, 2013
Delayed puberty and estrogen resistance in a woman with estrogen receptor α variantSamuel D Quaynor, Earl W Stradtman, Hyung-Goo Kim, et al.
American Journal of Obstetrics and Gynecology|April 23, 2005
Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarraysNing Xu, Robert H Podolsky, Pranav Chudgar, et al.
Journal of Assisted Reproduction and Genetics|December 23, 2025
The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndromeJaclyn M Kwal, Lynn P Chorich, Anna Navitski, et al.
Scientific Reports|December 29, 2019
The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic VariantsJ Graham Theisen, Viji Sundaram, Mary S Filchak, et al.
Pageof 3